Aesculap Implant Systems
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K121879 | VEGA KNEE SYSTEM | JWH | 2012-07-27 | View |
| 510(k) | K101815 | ENDURO KNEE SYSTEM | KRO | 2010-12-20 | View |
| 510(k) | K100623 | AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM | NKB | 2010-06-09 | View |
| 510(k) | K090299 | BIOLOX OPTION CERAMIC FEMORAL HEAD AND METHA XL HEADS | LZO | 2009-04-24 | View |
| 510(k) | K090657 | MODIFICATION TO: S4 SPINAL SYSTEM | NKB | 2009-04-20 | View |
| 510(k) | K071945 | S4 SPINAL SYSTEM | NKB | 2007-09-20 | View |
No matching devices.
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